Arvidsson 2005.
Methods | computer randomisation | |
Participants | 100 women randomised; age and gestational ages averages not given; included gestational age up to 49 days confirmed by ultrasound; exclusion criteria: contraindications for medical abortion.Setting: Karolinska Hospital, Sweden | |
Interventions | mifepristone 600mg (all) followed 36‐48 hrs later by: group1) misoprostol 400mcg oral group 2) misoprostol 800mcg vaginal |
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Outcomes | experience of pain, occurrence of side‐effects, duration of bleeding | |
Notes | 10 women could not be reached by phone 3‐7 weeks after abortion; 30 women did not agree or weren't asked to be called during this time frame |